Give the product and mechanism of the reaction of 1-(tert-butyl)-1-cyclohexene with ethanol. Product: Mechanism:

Q: Writethe mechanisms for each of the following reactions and briefly comment on the expected product…

A:

Q: What product would you expect to obtain from addition of Cl2to 1, 2-dimethylcyclohexene? Show the…

A: Addition reaction of Alkene with halogens: When an alkene reacts with halogens like Cl2 and Br2 in…

Q: Draw the structures of the intermediate bromonium and cyclic carbocation and propose mechanisms for…

A: Solution- The structures of the intermediate bromonium and cyclic carbocation is shown as follows:

Q: Draw the structures of two stereoisomeric alkenes that would give 3-hexanol or hexan-3-ol as the…

A:

Q: a) Provide a mechanism that accounts for the product formed in the following reaction. OH CH +…

A: In both the reactions, carbocation rearrangement takes place through hydride shift

Q: For the reaction, give the expected substitution product:   a) 1-iodo-1-methylcyclohexane +…

A:

Q: A ketone undergoes acid-catalyzed bromination, acid-catalyzed chlorination, racemization, (see page…

A:

Q: Give the reaction mechanism showing all possible products for the following reactions: (a) Reaction…

A:

Q: Below is a series of electrocyclic reactions from compounds A to B, to C and finally to D under…

A: a. See the structures of B and C below. b. step 1: 6 pi electron system, thermal, dis rotation is…

Q: What product(s) would you expect from reaction of (S)-3-chloro-3methyloctane with acetic acid? Show…

A: Please find  attached the answer in handwritten note.

Q: 1. NaOH, I2 2. H30* 1. NaOCH2CH3 + OCH,CH3 2. H2О ELOH

A: Acid anhydrides react with alcohols to form esters.     it is iodoform reaction

Q: Give the major product of the following reaction. -? Br2

A: The major product of the reaction has to be given

Q: On ozonolysis of 1,3,5-trimethyl benzene will give a. C6H5COCHO b. CH3COCHO с. СНО-СНО d. CH3COCOCH3

A: Three moles of butan-2,3-one will be formed

Q: How many alkenes yield 2,2,3,4,4−pentamethylpentane on catalytic hydrogenation?

A: In the given compound, double bond is only possible at C3 because C2 and C4 are the 30 carbon.

Q: Predict what the monohalogenation major product(s) will be from the chlorination of isooctane. CH,…

A: Alkanes are less reactive however inpresence of sunlight conditions they undergo free radical…

Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: When 5-bromo-1-pentanol is treated with sodium hydride in diethyl ether, the product is analyzed to…

A: The reaction that involves the substitution of a group (leaving group) by the incoming electron-rich…

Q: 2,3-Dimethylbutane reacts with bromine in the presence of light to give a mono brominated product.…

A: 2,3-dimethylbutane reacts with bromine in the presence of light to give a mono brominated product.…

Q: conc. Br Ph HBr (aд) Н-Br Ph Ph (-) Br Br Ph mixture of E/Z isomers ®¸Ph mixture of E/Z isomers

A:

Q: CHO 3C CH3 CHO + NaOH, H2O → ? NaOH, H,O CH3 (CH3)₂CHCHO ? NaOH, H,O ?

A:

Q: Carbocations undergo 1,2-methyl shift or 1,2-hydride shift to produce a more stable intermediate.…

A: The mechanism can be shown as:

Q: Propose a mechanism for addition of HI to 1-methylcyclohexene to give 1-iodo1-methylcyclohexane.…

A: Interpretation: A mechanism for addition of HI to 1-methylclohexane to give…

Q: What product would you expect from the reaction of the following with aqueous acidic KMNO,? a.…

A: Answer - (b)

Q: ОН to CF3CO,H

A:

Q: How many alkenes yield 2,3−dimethylbutane on catalytic hydrogenation?

A: Two alkenes on catalytical hydrogenation yields 2,3-dimethyl butane.

Q: The reaction of (2S)-2-chloro-3-methylpentane with sodium iodide yields two products:…

A: In SN-2 mechanism, usually inversion of configuration occurs because nucleophile attacks from…

Q: H;C,. 13C, + enantiomer CH3 H3C

A: The reaction given is,

Q: 2. Propose mechanisms for the following reactions: Cl- substitution in [(n²-C2H4)PtCl3]* by Br in…

A: Explained as follows

Q: What product(s) would you expect from reaction of (S)-3-chloro-3- methylheptane with acetic acid?…

A: This is an example of SN1 reaction because carbocation is tertiary and solvent is polar-protic.

Q: Why do both the following alkenes yield the same product upon reaction with hydrobromic acid?…

A:

Q: In the presence of acid such as H2SO4, 3,4-dimethyl-1-pentene undergoes isomerization to…

A: Alkene has a double bond present in the molecule. Hence alkenes are electron rich. Hence they take…

Q: ) Give the product and the type of mechanism of the reaction of hydrosulfide (HS¯) with (R)-…

A:

Q: CH3 Ill CH₂ H Br NC. NaOEt, EtOH CH3 NBS luz D NaOCH3 CH3OH ? H3O*, A E

A: Here we have to predict the major product formed in the following given reactions.

Q: When 3-bromo-1-methylcyclohexene undergoes solvolysis in hot ethanol, two productsare formed.…

A: The overall reaction for the given reaction is, The mechanism for the above reaction can be shown…

Q: (a) Give a mechanism for this reaction, showing how the two products arise as aconsequence of the…

A: a.

Q: OCH3 LOH

A:

Q: Consider the substitution reaction that takes place when (R)-3-bromo-3-methylhexane is treated with…

A: The reactant given is (R)-3-bromo-3-methylhexane.

Q: why do (R)-3-chloro-1-methylcycloprop-1-ene and 5-Bromo-1,3-Cyclohexadiene react differently with…

A:

Q: 1. For each one of the following reactions, show step by step mechanism of the reactions and…

A: NOTE: please note according to our policy , we can only answer first three subparts of a question.…

Q: Predict the product and give the stereochemistry resulting from reaction of each of the following…

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Q: Predict the elimination products of the following reactions, and label the major products.(a)…

A: The elimination reaction of cyclohexane is proceeded by chair conformer of cyclohexane to get the…

Q: In a hydrogenation reaction, cyclohex-1, 3-diene will be converted to

A: Hydrogenation means addition of Hydrogens.

Q: What stereochemistry would you expect for the alkene obtained by E2 elimination of…

A: The E2 elimination takes place in most of the cases in anti periplanner orientation . And occurs in…

Q: Give the structure and predict the stereochemistry of the major product formed in each of the…

A:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.